Clinical Research Associate Ii-zhengzhou

Parexel

Zhengzhou, China
Fully remote
Implement and monitor clinical trials
Ensure compliance with regulatory requirements
Perform source document verification
At Parexel, we are committed to improving the world's health through clinical development solutions

Job Summary

  • At Parexel, we are committed to improving the world's health through clinical development solutions.
  • The role involves assessing investigative sites and ensuring compliance with ICH GCP guidelines.
  • Team members work collaboratively to resolve trial issues and facilitate timelines.

Matching Summary

At Parexel, we are committed to improving the world's health through clinical development solutions.

Skills & Requirements

Must-have

  • Implement and monitor clinical trials
  • Ensure compliance with regulatory requirements
  • Perform source document verification

Nice-to-have

  • Mentor junior-level CRAs
  • Facilitate audits and audit resolution
  • Strong communication skills

Key Requirements

  • Experience in clinical trials
  • Knowledge of ICH GCP guidelines
  • Ability to communicate with investigative sites

Work Rights

Not specified

Tailored Resume

Cover Letter